A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040798



Internal ID94914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118373828..118379177hg38UCSC Ensembl
chr10:120133340..120138689hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg385350
hg195350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497395
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040798
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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